SBIR-STTR Award

Genetic and metabolic probes of antibiotic resistance
Award last edited on: 12/2/02

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$510,832
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Gerard Cangelosi

Company Information

Micro-Probe Corporation (AKA: Microprobe~Saigene~Epoch Pharmaceuticals~Epocj Bioscience)

1725 220th Street SE Suite 104
Bothell, WA 98021
   (425) 485-8566
   N/A
   N/A
Location: Single
Congr. District: 01
County: Snohomish

Phase I

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1993
Phase I Amount
$48,220
The ahn is to evaluate a novel technology for testing the susceptibility of prokaryotes to certain antibiotics. Our goal is to develop rapid antibiotic susceptibility tests for Mycobacterium tuberculosis and other pathogens. The technology will rapidly detect growth of resistant bacteria challenged with antibiotics in pure of mixed cultures, using oligonucleotide probes for two RNA targets: ribosomal RNA precursors (pre-rRNA), and mature ribosomal RNA (rRNA). Cellular copy number of pre-rRNA sequences are very sensitive to rifampicin, declining rapidly upon exposure from high to undetectable levels. By probing for these sequences in cells challenged briefly with rifampicin, it will be possible to detect growing (resistant) cells in a single measurement. Mature rRNA has species-specific sequences useful for detection of bacteria in mixed cultures containing other species. Probes for mature rRNA will be combined with probes for pre-rRNA in a rapid, sensitive, easv-to-use assay that simultaneously identifies bacterial species in primary enrichment cultures and determines their susceptibility to rifampicin and other antibiotics. Such a test would predict the outcome of antibiotic treatment much more rapidly and accurately than conventional tests. In Phase I, we will test the feasibilitv of the concept using a fast-growing, well characterized bacterium, Escherichia coli. Experiments will focus initially on resistance to rifampicin, one of the "first-line" antibiotics for treatment of tuberculosis, and then on other antibiotics. In Phase 11, we will transfer the technology to the more challenging Mycobacterium tuberculosis system. Ultimately, we will apply the technology to other climcally important microorganisms as well.Awardee's statement of the potential commerctal applications of the research: The technology would be incorporated into rapid, sensitive, easy-to-use antibiotic susceptibility tests for tuberculosis and other infectious diseases. Such tests would glve results much faster than conventional culture methods, and would allow specific detection of antibiotic-resistant species even in the presence of other bacterial species, regardless of their susceptibility. This would be a significant aid to clinicians attempting to predict the outcome of antibiotic treatment.National Institute of Allergy and Infectious Diseases (NIAID)

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
1994
(last award dollars: 1995)
Phase II Amount
$462,612

We will develop a suite of rapid, reliable, semiautomated DNA probe assays for antibiotic-resistant Staphylococcus species responsible for a variety of nosocomial infections. First, we will develop a DNA probe test for the mecA gene of methicillin-resistant S. aureus (MRSA) and coagulase-negative Staphylococcus species (MRCNS). The mecA gene codes for methicillin resistance in 97% to 100% of MRSA and MRCNS isolates. Direct detection of mecA will be more rapid, accurate, and reliable than current culture-dependent methicillin susceptibility tests, which are compromised by highly variable expression of the resistance phenotype in vitro. The DNA probe test will also include probes for identification of individual Staphylococcus species, allowing simultaneous species ID and detection of methlcillin resistance in a single test. The test will be conducted on colonies picked from primary isolation plates, and will require only 15 minutes of manual processing followed by 35 minutes of automated processing, yielding results in under I hour. We will also develop assays for resistance to second-line antibiotics used to treat MRSA and MRCNS infections. These tests will be conducted on isolates confirmed to be methicillin resistant by the combined mecA/species assay, and will require 2-4 hours to obtain results with under 30 minutes of manual processing. The entire suite of assays will yield complete species ID and antibiotic susceptibility results within half a day of picking colonies from plates.Awardee's statement of the potential commercial applieations of the research:Antibiotic susceptibility tests are conducted on most or all Staphylococcus infections. The technology will improve on the reliability of current tests, and make results available 24-48 hours sooner. Therefore, all clinical microbiology laboratories carrying out susceptibility testing stand to benefit by adopting the proposed technology.National Institute of Allergy and Infectious Diseases (NIAID)